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Snail family transcriptional repressor 2 mRNA 3′ untranslated region (SNAI2 mRNA 3′UTR)

Target
SNAI2 mRNA 3′UTR
Molecular classification
RNA, mRNA regulatory region
01

Overview

The SNAI2 mRNA 3′ untranslated region (3′UTR) is a critical regulatory segment of the messenger RNA encoding the Snail family transcriptional repressor 2, also known as Slug (UniProt: O43623). This region contains multiple binding sites for microRNAs (miRNAs) and RNA-binding proteins that control the stability and translation efficiency of the SNAI2 transcript. SNAI2 is a master regulator of the epithelial-mesenchymal transition (EMT), a process essential for embryonic development but frequently hijacked by cancer cells to promote invasion, metastasis, and resistance to therapy (PMID: 23568941). By targeting the SNAI2 mRNA 3′UTR with miRNA mimics or antisense oligonucleotides, researchers aim to suppress SNAI2 expression and reverse the EMT phenotype in aggressive tumors. Endogenous miRNAs such as miR-1, miR-124, and miR-203 naturally bind to this region to downregulate SNAI2, and their loss is often associated with poor prognosis in various malignancies (PMID: 21460138, PMID: 23873011). Consequently, this regulatory region represents a promising therapeutic target for preventing cancer progression and overcoming chemoresistance through RNA-based interventions.

Other names
SLUG mRNA 3′UTRSnail2 3′UTRSNAI2 3′-untranslated regionSLUG 3′-UTR
02

Mechanism of action

Binding of complementary RNA sequences, such as microRNA (miRNA) mimics or antisense oligonucleotides (ASOs), to specific seed sequences within the 3′UTR leads to the recruitment of the RNA-induced silencing complex (RISC), resulting in mRNA degradation or translational inhibition of the SNAI2 transcript (PMID: 20802496, PMID: 21460138).

03

Biological functions

Regulation of gene expressionmRNA stabilityTranslation regulationEpithelial-mesenchymal transition (EMT)Cell migrationNeural crest cell development
04

Disease associations

CancerMetastasisFibrosisChemoresistanceWaardenburg syndrome type 2D (via gene mutations)
05

Safety considerations

Off-target silencing of other mRNAs sharing similar seed sequencesPotential interference with normal developmental processes involving neural crest cellsSystemic delivery challenges and potential for innate immune activation by synthetic RNAsRisk of affecting wound healing processes where EMT is physiologically required
06

Interacting drugs

miR-203 mimics (experimental)

5 more in the full profile.

07

Biomarkers

SNAI2 protein expression levelsE-cadherin (CDH1) downregulationVimentin (VIM) upregulationmiR-203 expression levelsCirculating tumor cells (CTCs) with EMT markers

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